Canonical Allele Identifier: CA342628634

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437765C>A (hg19) ; chr1:g.154465289C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465289C>A , CM000663.2:g.154465289C>A	GRCh38
NC_000001.10:g.154437765C>A , CM000663.1:g.154437765C>A	GRCh37
NC_000001.9:g.152704389C>A	NCBI36
NG_012087.1:g.65097C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1316C>A MANE Select	ENSP00000357470.3:p.Ser439Tyr
ENST00000344086.8:c.*124C>A	ENSP00000340589.4:n.*124C>A
ENST00000368485.7:c.1316C>A	ENSP00000357470.3:p.Ser439Tyr
ENST00000507256.1:n.514C>A
NM_000565.3:c.1316C>A	NP_000556.1:p.Ser439Tyr
NM_181359.2:c.*124C>A	NP_852004.1:n.*124C>A
XM_005245139.1:c.1080C>A	XP_005245196.1:p.Val360=
XM_005245140.1:c.*157C>A	XP_005245197.1:n.*157C>A
XM_006711298.1:c.1364C>A	XP_006711361.1:p.Ser455Tyr
XM_005245139.2:c.1080C>A	XP_005245196.1:p.Val360=
XM_005245140.3:c.*157C>A	XP_005245197.1:n.*157C>A
XM_006711298.2:c.1364C>A	XP_006711361.1:p.Ser455Tyr
XM_017001199.2:c.1463C>A	XP_016856688.1:p.Ser488Tyr
XM_017001200.2:c.1415C>A	XP_016856689.1:p.Ser472Tyr
XM_017001201.2:c.*157C>A	XP_016856690.1:n.*157C>A
NM_000565.4:c.1316C>A MANE Select	NP_000556.1:p.Ser439Tyr
NM_181359.3:c.*124C>A	NP_852004.1:n.*124C>A
NM_001382769.1:c.1415C>A	NP_001369698.1:p.Ser472Tyr
NM_001382770.1:c.1409C>A	NP_001369699.1:p.Ser470Tyr
NM_001382771.1:c.1364C>A	NP_001369700.1:p.Ser455Tyr
NM_001382772.1:c.1310C>A	NP_001369701.1:p.Ser437Tyr
NM_001382773.1:c.*124C>A	NP_001369702.1:n.*124C>A
NM_001382774.1:c.956C>A	NP_001369703.1:p.Ser319Tyr